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平滑肌肉瘤:三例含有结蛋白阳性肿瘤细胞,缺乏平滑肌细胞的超微结构特征。

Leiomyosarcomas: three cases with desmin positive tumour cells, lacking ultrastructural features of smooth muscle cells.

作者信息

Roholl P J, de Jong A S, Albus-Lutter C E, van Unnik J A

机构信息

Institute for Pathology, Utrecht, The Netherlands.

出版信息

Histol Histopathol. 1988 Oct;3(4):389-94.

PMID:2980248
Abstract

A combined study of light and electron microscopy and of immunolabelling of three pleomorphic spindle cell sarcomas is presented. The light and electron microscopic features of these sarcomas were most compatible with those described for malignant fibrous histiocytoma (MFH, pleomorphic-storiform subtype). Electronmicroscopically undifferentiated and fibroblast-like cells, fibrohistiocytes and multinucleated histiocytes were observed. Characteristics belonging to smooth muscle cells were absent. By immunostaining, vimentin and desmin could be observed in tumour cells of all three cases, at least on frozen sections. Other markers such as alpha 1-antichymotrypsin, S-100 proteins, laminin, collagen IV and markers specific for skeletal muscle cells (myoglobin, actin and myosin specific for skeletal muscle) could not be demonstrated. These findings indicate that three MFH's are, in fact, poorly differentiated variants of smooth muscle tumours. It is concluded that immunophenotyping is very useful for this type of neoplasm.

摘要

本文呈现了一项对三种多形性梭形细胞肉瘤进行光镜、电镜及免疫标记联合研究的结果。这些肉瘤的光镜和电镜特征与恶性纤维组织细胞瘤(MFH,多形性-席纹状亚型)所描述的特征最为相符。电镜下观察到未分化细胞、成纤维细胞样细胞、纤维组织细胞和多核组织细胞。未观察到属于平滑肌细胞的特征。通过免疫染色,在所有三例病例的肿瘤细胞中至少在冰冻切片上可观察到波形蛋白和结蛋白。其他标志物如α1-抗糜蛋白酶、S-100蛋白、层粘连蛋白、IV型胶原以及骨骼肌细胞特异性标志物(骨骼肌特异性肌红蛋白、肌动蛋白和肌球蛋白)均未被证实。这些发现表明,这三种MFH实际上是平滑肌肿瘤的低分化变体。结论是免疫表型分析对这类肿瘤非常有用。

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